How to go back to same old, same old?
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seashell...Having been on these boards for several years now...and having had my own rather significant transformation resulting from bc and treatment, I can say that a vast majority of us seem to go through certain stages after treatment finally ends. Though our journeys are as individual as we, ourselves, are, they do seem to have some commonalities. Immediately following the end of treatment, many of us experience a sort of post-traumatis stress reaction, characterized by everything ranging from panic at being "left flapping in the wind" and terrified of recurrence, to depression and feelings of powerlessness, to a need to exercise our personal power and have some sort of giant impact of the world. For me, I felt, at first, very alien among others, full of new self-knowledge and a rising desire to make my life more meaningful, while among people who seemed, to me, content with the status quo and what I saw as inane, rote activity. I was truly antsy and wanted to really "break out." Unfortunately, I couldn't find much direction for this new energy and, so, "settled for" getting to know myself better and trying to identify, really, what I wanted my life to be about. Somehow, the experience of having your life threatened, as we've had, prompts us to the realization that this is, indeed, NOT a dress rehearsal and if we have just this one go-around, we'd better make it a good one! Anyway, for, me, it's 3 1/2 years later and I can see that through persistent efforts to become more authentic and make my life fuller and more meaningful, I have succeeded in achieving a satisfying, sometimes exciting, generous life and have even begun to learn what true, deep human love is all about. I'd still like to ditch my job and establish a wellness center in the mountains, volunteer with rescued animals, donate more money to several charities that I care about, and travel to every place in the world that holds fascination for me. And maybe I will do some or all of those things. But for now, I'm content. And having been one of the most disgruntled persons you can imagine, pre-bc, I'd say that that's a freakin' miracle!
I guess what I'm saying to you, seashell, is that the way you're feeling is super-healthy and very exciting. Don't let up on your desires. Maybe your husband never will join you on any of your new adventures, but that doesn't mean you won't have them. Maybe you can even start planning one right now. But also be gentle with yourself and, as they say, remember to "stop and smell the flowers"...because I'm betting that your olfactory senses, like many of your other means of exploring the world, have been vastly heightened as a result of the journey you've been on!
~Marin
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I had the same problem. when I finished my treatment it seemed like all my family had this attitude of yeahh you've finished, now whats for dinner?

I WAS doing all the things before my BC diagnosis. I'm a stay at home mom with a 3 year old and we all know life does not stop for young kids. I was doing all the running around that comes with being a stay at home mom. BUT...I was with myself inside. I would cry when I was driving, in the washroom when my daughter was having a nap. I thought that it would get better as the days..weeks..months went on. I didn't.
Then early January of this year I went to my family doctor for me yearly "check". She could tell something was wrong. I let everything out, she then told me,"you don't need to be suffering like this.I wish you came to me sooner."
She recommended a low dose of Effexor. I must admitt I was hesitant to take MORE meds just going through treatment and all, but I needed something was at my wits ends. I gave in..and it's been over 3 months now. I feel soooo much better. The weepy feelings are gone. I have not cried. Doing the daily "chores" are somewhat enjoyable. But most importantly I have moved on from all of this and am enjoying my life.
*..LOL, it seems like there has been a lot of depression discussion lately on the boards and I keep talking about Effexor. I should be one of their company reps! *
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good for your doc in recognizing your need for meds! and good for you for taking care of yourself.
When I was a year out from dx, I totally remodelled my home---redecorated, painted, removed paneling, etc, etc. I figured I''d waited long enough and who the hell knew if I'd have time to do it later?
Fortunately, my dh and I had begun travel after our 25th anniv and kept it up---so have done most of that that I wanted to do---now, I do the things I WANT to do---and yes, I do them alone, cause he is not interested---but I've found that there are a lot of places to go and things to do with women who have an adventureous streak.
Whitewater rafting, Sweet Potato Queens weekend, pool training, craft fairs,chick movies, theater, you name it and I will sign on for it, and likely make the reservations. I have FINALLY discovered that I don't need my spouse to go along with me -- I'm not responsible for his fun, only my own.
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Thats the one thing I wish to start doing is travelling. And good for you Iodine for going on vacation solo!!!!
When I was going through chemo, I was sick and tired of the paint color in my condo. So on Christmas...yes Christmas we painted...lol. I was able to use the cancer card to get out of functions so it worked out. Later on I completely went through everything, i mean everything and re decorated. First thing was a new Plasma...and leather ottoman.
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Hello!
Thanks so much to all for your feedback! I had to laugh...there seems to be a similiar thread of all of us "cleaning out & redecorating" post bc. My New Year's resolution was to clean out my entire house and redecorate several areas. It has been a huge job but I have finally had the energy to do it! (even with my painful Arimidex hands!)
Marin, Thank you for taking the time to write ALL of that. It was great and validating! You described the bc journey so well, and the "after effects." I definitely am at the stage of antsy and want to break out stage! It has been a long winter of "cleaning out the house" (I'm almost done!)...but I'm ready for what's next that is fulfilling and meaningfull! You are so right about "stopping and smelling the roses" ~ I now take the time to enjoy the beauty of the blossoms on the Dogwoods, tossing a "helicopter" seed into the air and watch it spin down etc. I really appreciate your thoughts and advice!!

Lexislove, I am so glad you are doing well on Effexor. Being home with little ones you really can't make alot of changes, your family just needs you! My Dr. actually offered me Effexor for my hot flashes but I was like you... more meds? Still thinking about it... (love the baby pict on your avatar!)

Iodine, Love your advice! I was actually thinking of getting a few friends together to start a Fun Club who would enjoy some of the adventures I have in mind! Good ideas!!
Off to plan a fun outing for the day!!!!

I wish you all a great day!!!
Sue xo
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Hi Seashell,
It has been barely 6 months since my operation and emotions have been running high. At first I was on a roller coaster ride. During radiation I felt "safe" as doctors and nurses were soo sweet but then I was on my own. A phonecall to Hospice made me feel that it's ok to feel that way but that I needed to move on. What really helped me (apart from support from my dear husband, children, parents, relatives and friends) was visualising what I'd like to do as i healed post op. For me, that meant gaining enough strenght to exercise at the gym as previously. (I love fitness sessions, aerobics etc etc). Somehow I was energised enough to go uphill carrying with me rebellion. I used to look up resilient people on the Internet and learn from their qualities. Thankfully, this BC has made me stronger. I've gained back my strength and energy and like you feel this need to have more fun!!! and to live life to the full. I'm also aware of chances of recurrence. But "live a little, or die a little?" We're doing everything we can to stay healthy.
Take care.
Katee
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Oh boy Katee - no one has told you the "new normal"?
Okay for you normal is the way you were before diagnosis. However, you have to alter your definition as various side effects are permanent. An example is lymphadema. Once your arm swells, there may be no getting back to the place you once were. You can only move foreward. If you dont mind, I will start:
I hope that you will be able to accept and love yourself just as you are now. I hope that you are proud enough of us to invite to meet the other branch of the family. If you live and love - then all should work out because everyone will take care of everyone else. The family you want and need are right there hoping you will ask for their support.
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Hi Katee,
Thanks for your feedback! I can totally relate to what you were feeling when you finished rads. I can remember when I finished my treatments... I felt the same way, safe while I was getting them and such a let down when it was over. I had myself so physched up for it... it was like..now what? I like your ideas of visualizing what I want to do next..and gaining positive energy from inspiring people!! I just get frustrated when everyone around me wants to go back to the old routine... I feel a sense of urgency like I need to "do it now" and not wait 'til I'm 65!? I decided to tackle cleaning out my entire house this winter... I should have selected something a bit more fun!! I'm almost done..and summer is nearly here... so then I will have FUN!!
Have a great weekend!!

Sue
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